A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036411



Internal ID20603451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:52863401..52864000hg38UCSC Ensembl
chr17:50940761..50941360hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524597
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036411
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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